PERCOCET is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Mckesson Rxpak Inc. The primary component is Oxycodone Hydrochloride; Acetaminophen.
Product ID | 65084-298_81152a6d-7c01-432e-a811-f3ffb00435fa |
NDC | 65084-298 |
Product Type | Human Prescription Drug |
Proprietary Name | PERCOCET |
Generic Name | Oxycodone Hydrochloride And Acetaminophen |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 1999-06-30 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA040330 |
Labeler Name | Mckesson Rxpak Inc |
Substance Name | OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN |
Active Ingredient Strength | 5 mg/1; mg/1 |
Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 1999-06-30 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA040330 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1999-06-30 |
Marketing End Date | 2019-09-05 |
Ingredient | Strength |
---|---|
OXYCODONE HYDROCHLORIDE | 5 mg/1 |
SPL SET ID: | 66a32123-df98-43fe-8c8a-e153bc3b0c07 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
63481-623 | PERCOCET | oxycodone hydrochloride and acetaminophen |
63481-627 | PERCOCET | oxycodone hydrochloride and acetaminophen |
63481-628 | PERCOCET | PERCOCET |
63481-629 | PERCOCET | PERCOCET |
63629-3773 | PERCOCET | PERCOCET |
63629-3776 | PERCOCET | PERCOCET |
65084-298 | PERCOCET | PERCOCET |
0406-0512 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen |
0406-0522 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen |
0406-0523 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen |
0603-4978 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
0603-4979 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
0603-4982 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
0603-4998 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
0904-6437 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
0904-6438 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
0904-6439 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
10544-287 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen |
21695-233 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen |
21695-616 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
52959-556 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
55700-983 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen |
55700-984 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen |
63187-406 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen |
29033-405 | Oxycodone Hydrochloride and Acetaminophen | Oxycodone Hydrochloride and Acetaminophen |
46672-648 | oxycodone hydrochloride and acetaminophen | oxycodone hydrochloride and acetaminophen |
60760-200 | Oxycodone Hydrochloride and Acetaminophen | Oxycodone Hydrochloride and Acetaminophen |
23635-115 | Xartemis | oxycodone hydrochloride and acetaminophen |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PERCOCET 73072165 1051682 Live/Registered |
ENDO LABORATORIES, INC. 1975-12-18 |